Z-1044-2014 Class II Terminated
Recalled by Zimmer, Inc.
— Warsaw, IN
FDA device recall Z-1044-2014 was initiated by Zimmer, Inc. on Oct 11, 2013 and is designated Class II. Reason for recall: Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. (ZMBV) facility in Ponce, Puerto Rico. Based on this review, it was determined that the… The recall status is terminated (terminated Apr 14, 2017). Affected quantity: 7,044,680 total.
Recall Details
- Product Type
- Devices
- Report Date
- Feb 26, 2014
- Initiation Date
- Oct 11, 2013
- Termination Date
- Apr 14, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 7,044,680 total
Product Description
3.5 X 10 CORT SCREW SELFT 3.5 X 12 CORT SCREW SELFT 3.5 X 14 CORT SCREW SELFT 3.5 X 16 CORT SCREW SELFT 3.5 X 18 CORT SCREW SELFT 3.5 X 20 CORT SCREW SELFT 3.5 X 22 CORT SCREW SELFT 3.5 X 24 CORT SCREW SELFT 3.5 X 26 CORT SCREW SELFT 3.5 X 28 CORT SCREW SELFT 3.5 X 30 CORT SCREW SELFT 3.5 X 32 CORT SCREW SELFT 3.5 X 34 CORT SCREW SELFT 3.5 X 36 CORT SCREW SELFT 3.5 X 38 CORT SCREW SELFT 3.5 X 40 CORT SCREW SELFT 3.5 X 45 CORT SCREW SELFT 3.5 X 50 CORT SCREW SELFT 3.5 X 55 CORT SCREW SELFT 3.5 X 60 CORT SCREW SELFT 3.5 X 75 CORT SCREW SELFT
Reason for Recall
Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. (ZMBV) facility in Ponce, Puerto Rico. Based on this review, it was determined that the packaging operations conducted in the Building 1 packaging operation at this facility were not properly validated. As a result, Zimmer conducted seal integrity testing to evaluate if previously packaged product from this facility met the established requirements for sterile barrier integrity. The acceptance criteria established for this testing was 99% reliability with a 90% confidence interval. These packaging tray configurations met the acceptance criteria for sterile barrier integrity of both the inner and outer trays, however, Zimmer has decided to recall all manufacturing lots that have not expired and that were sterile packaged in the ZMBV facility Building 1 packaging operations.
Distribution Pattern
Worldwide Distribution-USA (nationwide) and the countries of Belgium, Canada, Canary Islands, China, Czech Republic, Denmark, Finland, France, Germany, Greece, India, Italy, Japan, Korea, Luxemburg, Netherlands, New Zealand, Norway, Portugal Reunion, Russian Federation, Singapore, Slovakia, Spain, Sweden, Switzerland, Turkey, Taiwan, Thailand, and United Kingdom.
Code Information
61173204 61173205 61173206 61804309 61173207 61804310 61173208 61117130 61173210 61173212 61173213 61173214 61173215 61173216 61173218 61173219 61173220 61173221 61173223 61173224 61173226 61173228 61173231
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1044-2014
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026
These dates say when openFDA published the data file and when RegDataLab last loaded it.